HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064022Generated: October 30, 2026
1-Hydroxybenzotriazole → HCID 59140113, compound
https://huagongshe.com/reaction/2064022
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | O-(2-(Vinyloxy)ethyl)hydroxylamine | HCID 21867017 | — |
| Reactant | 5-(4-Bromo-2-fluorophenylamino)-imidazo[1,5-a]pyridine-6-carboxylic acid | HCID 59140163 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59140113 | HCID 59140113 | 53.6% |
Reaction Steps
To a solution of 5-(4-Bromo-2-fluorophenylamino)-imidazo[1,5-a]pyridine-6-carboxylic acid (2.0 g, 5.7 mmol) and O-(2-vinyloxyethyl)-hydroxylamine (0.71 g, 6.8 mmol) in DMF (44 mL) was added EDCI hydrochloride (1.42 g, 7.41 mmol), HOBt (1.0 g, 7.41 mmol) and DIPEA (0.97 mL, 5.69 mmol). The reaction mixture was stirred at room temperature for 3 hours before being concentrated in vacuo. The resultant residue was dissolved in 1:1 diethylether:ethyl acetate (30 mL) and aqueous saturated sodium hydrogen carbonate solution (30 mL) was added. The resultant mixture was sonicated until a precipitate formed. The precipitate was collected by filtration and washed with 1:1 diethylether:ethyl acetate to yield the title compound as a tan solid (1.33 g, 53%). LCMS (Method B): RT=2.78 min, M+H+=435/437.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288408B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-6caeae3b7b6c4ab2830a5642d40817d9 |
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| Source note | uspto-grants-2012_10 |
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